GRM5 glutamate metabotropic receptor 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 34 |
Likely benign | 0 | 54 |
association | 0 | 2 |
not provided | 0 | 2 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
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0 |
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0 |
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6 |
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166 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | GPRC1E |
SYNONYM | MGLUR5 |
SYNONYM | PPP1R86 |
SYNONYM | mGlu5 |
MIM | 604102 OMIM |
HGNC | HGNC:4597 HGNC |
Ensembl | ENSG00000168959 Ensembl |
AllianceGenome | HGNC:4597 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000455756.6 | hg38 | chr11 | 88,504,576 | 89,063,648 | 559,073 |
ENST00000305432.9 | hg38 | chr11 | 88,507,810 | 89,048,022 | 540,213 |
ENST00000393294.3 | hg38 | chr11 | 88,984,702 | 89,065,945 | 81,244 |
ENST00000305447.5 | hg38 | chr11 | 88,504,642 | 89,065,982 | 561,341 |
ENST00000455756.6 | hg19 | chr11 | 88,237,744 | 88,796,816 | 559,073 |
ENST00000305447.5 | hg19 | chr11 | 88,237,810 | 88,799,150 | 561,341 |
ENST00000305432.9 | hg19 | chr11 | 88,240,978 | 88,781,190 | 540,213 |
ENST00000393294.3 | hg19 | chr11 | 88,717,870 | 88,799,113 | 81,244 |
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